HRID274953

反应详情

EQUATION

反应方程式

HRID 274953 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
75 °C

PROCEDURE

实验过程

One hundred grams of 4,4'-dihydroxybenzophenone (0.467 mole) is added to 300 milliliters of ethanol in a stirred, 1-liter Erlenmeyer flask. After the 4,4'-dihydroxybenzophenone has dissolved, a solution consisting of 48.6 grams of hydroxylamine hydrochloride (0.699 mole) and 57.4 grams of sodium acetate (0.700 mole) in 70 milliliters of deionized water is added followed by an additional 100 milliliters of ethanol. This mixture is stirred and heated on a hot plate to a gentle refluxing condition (75° C.). After heating for 4 hours, the solution is allowed to cool to room temperature with stirring and then filtered. One hundred milliliters of ethanol is used to wash the filter cake. The total filtrant obtained (600.4 grams) is then concentrated to a weight of 219.2 grams by evaporation of the ethanol and water. This solution is then placed in a stirred 1-liter Erlenmeyer flask to which 600 milliliters of deionized water is added. With the addition of the deionized water, a white precipitate is formed. After 30 minutes of stirring, this solution is filtered. The solids obtained weigh 98.22 grams after drying. Sixty-six grams of this material (4,4'-dihydroxybenzophenone oxime, 0.288 mole) is added to 330 milliliters of glacial acetic acid in a 500 milliliter round bottom flask equipped with a stirrer, water cooled condensor, nitrogen purge and heating mantle. A catalytic amount of toluenesulfonic acid (1.85 grams, 0.027 mole) is next added and the reaction mixture is then heated to 83° C. After heating for approximately 2 hours, a precipitate is formed which is stirred for an additional 2 hours at 87° C. Twenty-five milliliters of deionized water is next added and after 30 minutes, the contents of the reaction flask are transferred to a stirred, 1-liter Erlenmeyer flask. Immediately following this transfer, 400 milliliters of deionized water is added. This solution is stirred for 45 minutes and then filtered. The filter cake obtained is washed with 800 milliliters of deionized water and then dried. The resultant solids, which are a light beige color, weigh 54.82 grams. Fourier transform infrared analysis of this product shows absorbances which are indicative of the structure for 4,4'-dihydroxybenzanilide. Differential scanning calorimetry analysis shows a sharp melt endotherm at 273° C. for the 4,4'-dihydroxybenzanilide thus obtained.

WORKUP

后处理

  1. additionis added
  2. temperatureAfter heating for 4 hours
  3. temperatureto cool to room temperature
  4. stirringwith stirring
  5. filtrationfiltered
  6. washto wash the filter cake
  7. customThe total filtrant obtained (600.4 grams)
  8. concentrationis then concentrated to a weight of 219.2 grams by evaporation of the ethanol and water
  9. additionis added
  10. additionWith the addition of the deionized water
  11. customa white precipitate is formed
  12. stirringAfter 30 minutes of stirring
  13. filtrationthis solution is filtered
  14. customThe solids obtained
  15. customafter drying
  16. customequipped with a stirrer
  17. customwater cooled condensor, nitrogen purge
  18. temperatureheating mantle
  19. temperaturethe reaction mixture is then heated to 83° C
  20. temperatureAfter heating for approximately 2 hours
  21. customa precipitate is formed which
  22. stirringis stirred for an additional 2 hours at 87° C
  23. additionis added
  24. stirringThis solution is stirred for 45 minutes
  25. filtrationfiltered
  26. customThe filter cake obtained
  27. washis washed with 800 milliliters of deionized water
  28. customdried
  29. customat 273° C.
  30. customthus obtained